IL266149B - קלציום קרבונט אמורפי לטיפול בלוקמיה - Google Patents
קלציום קרבונט אמורפי לטיפול בלוקמיהInfo
- Publication number
- IL266149B IL266149B IL266149A IL26614919A IL266149B IL 266149 B IL266149 B IL 266149B IL 266149 A IL266149 A IL 266149A IL 26614919 A IL26614919 A IL 26614919A IL 266149 B IL266149 B IL 266149B
- Authority
- IL
- Israel
- Prior art keywords
- composition
- acc
- acid
- leukemia
- stage
- Prior art date
Links
- 208000032839 leukemia Diseases 0.000 title claims description 61
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 title claims description 46
- 238000011282 treatment Methods 0.000 title claims description 28
- 229910000019 calcium carbonate Inorganic materials 0.000 title claims description 25
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 87
- 239000000203 mixture Substances 0.000 claims description 82
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- 208000010839 B-cell chronic lymphocytic leukemia Diseases 0.000 claims description 63
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- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 8
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
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- 229910052725 zinc Inorganic materials 0.000 description 3
- SJSQTARGNAQQKY-GBXIJSLDSA-N (2s,3r)-2-amino-3-sulfooxybutanoic acid Chemical compound OS(=O)(=O)O[C@H](C)[C@H](N)C(O)=O SJSQTARGNAQQKY-GBXIJSLDSA-N 0.000 description 2
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- HXXFSFRBOHSIMQ-FPRJBGLDSA-N alpha-D-galactose 1-phosphate Chemical compound OC[C@H]1O[C@H](OP(O)(O)=O)[C@H](O)[C@@H](O)[C@H]1O HXXFSFRBOHSIMQ-FPRJBGLDSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940093740 amino acid and derivative Drugs 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
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- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
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- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
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- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
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- 239000003085 diluting agent Substances 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- XWDLNPWILOXKHK-ALUAXPQUSA-L disodium [(2R,3S)-2,3-dihydroxy-4-oxopentyl] phosphate Chemical compound [Na+].P(=O)([O-])([O-])OC[C@H]([C@@H](C(C)=O)O)O.[Na+] XWDLNPWILOXKHK-ALUAXPQUSA-L 0.000 description 1
- VQLXCAHGUGIEEL-FAOVPRGRSA-L disodium;[(2r,3r,4s,5r)-2,3,4,5-tetrahydroxy-6-oxohexyl] phosphate Chemical compound [Na+].[Na+].[O-]P(=O)([O-])OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O VQLXCAHGUGIEEL-FAOVPRGRSA-L 0.000 description 1
- NTBQNWBHIXNPRU-MSQVLRTGSA-L disodium;[[[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-oxidophosphoryl] hydrogen phosphate;hydrate Chemical compound O.[Na+].[Na+].C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP([O-])(=O)OP(O)([O-])=O)[C@@H](O)[C@H]1O NTBQNWBHIXNPRU-MSQVLRTGSA-L 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
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- 238000013399 early diagnosis Methods 0.000 description 1
- 230000003028 elevating effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
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- 239000013505 freshwater Substances 0.000 description 1
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- 239000000499 gel Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000007407 health benefit Effects 0.000 description 1
- 230000008821 health effect Effects 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 230000036512 infertility Effects 0.000 description 1
- 239000007951 isotonicity adjuster Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000008297 liquid dosage form Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 208000003747 lymphoid leukemia Diseases 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 210000004962 mammalian cell Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- DWRVHDWKWKFSAI-UHFFFAOYSA-N methyl 3,4-difluorobenzoate Chemical compound COC(=O)C1=CC=C(F)C(F)=C1 DWRVHDWKWKFSAI-UHFFFAOYSA-N 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 210000005170 neoplastic cell Anatomy 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- 229950007002 phosphocreatine Drugs 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- MHXGNUVRVJWHJK-UHFFFAOYSA-N phosphono dihydrogen phosphate;sodium Chemical compound [Na].OP(O)(=O)OP(O)(O)=O MHXGNUVRVJWHJK-UHFFFAOYSA-N 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 150000004804 polysaccharides Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 description 1
- 235000019828 potassium polyphosphate Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002510 pyrogen Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical compound OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- ODFAPIRLUPAQCQ-UHFFFAOYSA-M sodium stearoyl lactylate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C([O-])=O ODFAPIRLUPAQCQ-UHFFFAOYSA-M 0.000 description 1
- 229940080352 sodium stearoyl lactylate Drugs 0.000 description 1
- YEQQMAFLJISSCR-UHFFFAOYSA-M sodium;1-carboxyethenyl hydrogen phosphate;hydrate Chemical compound O.[Na+].OC(=O)C(=C)OP(O)([O-])=O YEQQMAFLJISSCR-UHFFFAOYSA-M 0.000 description 1
- LXLBEOAZMZAZND-UHFFFAOYSA-M sodium;hydroxy-[1-hydroxy-3-[methyl(pentyl)amino]-1-phosphonopropyl]phosphinate Chemical compound [Na+].CCCCCN(C)CCC(O)(P(O)(O)=O)P(O)([O-])=O LXLBEOAZMZAZND-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007909 solid dosage form Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000213 sulfino group Chemical group [H]OS(*)=O 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- 125000002264 triphosphate group Chemical group [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- KWEUUBDPVVHQAL-MSQVLRTGSA-K trisodium;[[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O KWEUUBDPVVHQAL-MSQVLRTGSA-K 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/015—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/06—Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
- A61K33/10—Carbonates; Bicarbonates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/20—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/24—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- Nutrition Science (AREA)
- Hematology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Oncology (AREA)
- Physiology (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662412300P | 2016-10-25 | 2016-10-25 | |
| PCT/IL2017/051160 WO2018078616A1 (en) | 2016-10-25 | 2017-10-23 | Amorphous calcium carbonate for treating a leukemia |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL266149A IL266149A (he) | 2019-06-30 |
| IL266149B true IL266149B (he) | 2022-08-01 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL294615A IL294615A (he) | 2016-10-25 | 2017-10-23 | קלציום קרבונט אמורפי לטיפול בלוקמיה |
| IL266149A IL266149B (he) | 2016-10-25 | 2017-10-23 | קלציום קרבונט אמורפי לטיפול בלוקמיה |
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| IL294615A IL294615A (he) | 2016-10-25 | 2017-10-23 | קלציום קרבונט אמורפי לטיפול בלוקמיה |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US11052108B2 (he) |
| EP (1) | EP3532074B1 (he) |
| JP (1) | JP7152785B2 (he) |
| KR (1) | KR102531595B1 (he) |
| CN (2) | CN114948992A (he) |
| AU (1) | AU2017349921B2 (he) |
| IL (2) | IL294615A (he) |
| WO (1) | WO2018078616A1 (he) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| IL289237B2 (he) | 2019-07-23 | 2026-03-01 | Amorphical Ltd | קלציום קרבונט אמורפי לשיפור ביצועי ספורטאים |
| WO2021181372A1 (en) * | 2020-03-11 | 2021-09-16 | Amorphical Ltd. | Amorphous calcium carbonate for treatment of acidosis |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008041236A2 (en) * | 2006-10-05 | 2008-04-10 | Ben-Gurion University Of The Negev Research And Development Authority | Composition comprising crustacean gastrolith components, calcium carbonate and its use |
| WO2009053967A1 (en) * | 2007-10-22 | 2009-04-30 | Amorphical Ltd. | Stable amorphous calcium carbonate comprising phosphorylated amino acids, synthetic phosphorylated peptides, and gastrolith proteins |
| WO2014122658A1 (en) * | 2013-02-11 | 2014-08-14 | Amorphical Ltd. | Amorphous calcium carbonate for accelerated bone growth |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US4237147A (en) | 1974-01-04 | 1980-12-02 | Monsanto Company | Stabilized amorphous calcium carbonate |
| US4199496A (en) | 1974-09-05 | 1980-04-22 | Johnson Edwin L | Process for the recovery of chemicals from the shells of crustacea |
| EP0052677B1 (en) | 1980-11-21 | 1985-01-09 | Monsanto Company | Concentrates for the preparation of carbonated beverages |
| US4964894A (en) | 1986-03-31 | 1990-10-23 | Freepons Donald E | Plant growth regulators derived from chitin |
| DE3875867T2 (de) | 1987-08-28 | 1993-04-01 | Norwich Eaton Pharma | Kalziumzusaetze. |
| GB2217988B (en) | 1988-04-11 | 1992-04-01 | Gould Leonard W | Regimen for increasing bone density in humans |
| DE3853422T2 (de) | 1988-06-09 | 1995-10-26 | Innogenetics Nv | HIV-3-Retrovirus und seine Verwendung. |
| US5886012A (en) | 1989-03-22 | 1999-03-23 | Peter K. T. Pang | Method of treatment for disease associated with excessive PHF using combination therapy involving exogenous calcium and calcium channel blockers |
| US5037639A (en) | 1989-05-24 | 1991-08-06 | American Dental Association Health Foundation | Methods and compositions for mineralizing calcified tissues |
| US6348571B1 (en) | 1994-09-12 | 2002-02-19 | Northwestern University | Corticotropin release inhibiting factor and methods of using same |
| JPH099871A (ja) | 1995-07-03 | 1997-01-14 | Kita Nippon Shokuhin Kk | 菓 子 |
| WO1997024069A1 (en) | 1995-12-26 | 1997-07-10 | Holomed Aps | A method and system for generating an x-ray image |
| JPH10236957A (ja) | 1997-02-24 | 1998-09-08 | Bankaku Souhonpo:Kk | 骨粗鬆症の改善剤 |
| US20060165784A1 (en) | 1997-05-06 | 2006-07-27 | Zhao Jin R | Calcium supplement |
| SE9702401D0 (sv) | 1997-06-19 | 1997-06-19 | Astra Ab | Pharmaceutical use |
| US6569472B1 (en) | 2000-09-01 | 2003-05-27 | Wm. Wrigley Jr. Company | Coated chewing gum products containing antacid and method of making |
| US20030077604A1 (en) | 2000-10-27 | 2003-04-24 | Yongming Sun | Compositions and methods relating to breast specific genes and proteins |
| JP2002205947A (ja) | 2000-12-11 | 2002-07-23 | Chafflose Corporation | 水虫治療薬 |
| EP1416916B1 (en) | 2001-08-16 | 2007-10-17 | Cmp Therapeutics Limited | Chitin microparticles and their medical uses |
| JP2003292453A (ja) | 2002-04-02 | 2003-10-15 | Asahi Kasei Corp | 骨疾患治療用医薬複合剤 |
| JP2004081739A (ja) | 2002-08-29 | 2004-03-18 | Mitsuru Akashi | ハイドロキシアパタイト−ポリマー複合材料の止血用組成物 |
| KR20020082813A (ko) | 2002-09-06 | 2002-10-31 | 한국지질자원연구원 | 에탄올-에틸렌 글리콜계에서의 탄산화 반응을 이용하여제조된 비정질 탄산칼슘의 후처리 방법 |
| WO2005025581A1 (fr) | 2003-09-17 | 2005-03-24 | Third Military Medical University, Chinese People's Liberation Army, P.R. Of China | Utilisation de la n-acetyl-d-aminoglycosamine pour la preparation de medicaments de traitement du cancer et des metastases |
| GB0324918D0 (en) | 2003-10-24 | 2003-11-26 | Glaxo Group Ltd | Composition |
| KR100561231B1 (ko) | 2004-05-18 | 2006-03-15 | 한국지질자원연구원 | 표면개질에 의한 비정질 탄산칼슘 제조방법 |
| CA2567972C (en) | 2004-05-26 | 2015-07-28 | Ben-Gurion University Of The Negev Research And Development Authority | Orally-administrable compositions comprising stable amorphous calcium carbonate |
| WO2006043966A2 (en) | 2004-10-15 | 2006-04-27 | University Of Tennessee Research Foundation | Methods for inducing apoptosis in adipocytes |
| SG158153A1 (en) | 2004-12-21 | 2010-01-29 | Musc Found For Res Dev | Compositions and methods for promoting wound healing and tissue regeneration |
| CN101090949B (zh) | 2004-12-22 | 2013-06-05 | 索尔维公司 | 碱土金属碳酸盐的耐酸粒子 |
| DE102005047807A1 (de) | 2005-06-04 | 2006-12-07 | Solvay Infra Bad Hönningen GmbH | Modifizierte Nanopartikel |
| US20070041506A1 (en) | 2005-08-22 | 2007-02-22 | Michelle Bottino | Digital sensor holder |
| GB0522045D0 (en) | 2005-10-28 | 2005-12-07 | Novartis Ag | Pharmaceutical compositions |
| AU2007207429A1 (en) | 2006-01-19 | 2007-07-26 | Warsaw Orthopedic, Inc. | Injectable and moldable bone substitute materials |
| WO2009087553A1 (en) | 2008-01-02 | 2009-07-16 | Aurobindo Pharma Limited | Kits for administering bisphosphonates |
| CN101314031A (zh) | 2008-07-14 | 2008-12-03 | 王冰 | 一种改善骨营养的制剂 |
| EP2334292B1 (en) | 2008-10-17 | 2019-05-08 | Fresenius Medical Care Holdings, Inc. | Method of determining a phosphorus binder dosage for a dialysis patient |
| WO2010093285A1 (en) | 2009-02-12 | 2010-08-19 | Aduro Material Ab | Composition comprising biodegradable carrier for controlled drug delivery |
| CN101580260B (zh) | 2009-05-31 | 2011-04-27 | 河南大学 | 一种微乳液法制备无定形碳酸钙的方法 |
| EP2598579B1 (de) | 2010-07-30 | 2024-09-11 | Schaefer Kalk GmbH & Co. KG | Kugelförmige, amorphe calciumcarbonat-teilchen |
| CN103200938B (zh) | 2010-08-30 | 2018-07-31 | 普马特里克斯营业公司 | 干燥粉末配方及用于治疗肺部疾病的方法 |
| CN102085356B (zh) | 2010-12-28 | 2013-02-27 | 北京同仁堂健康药业股份有限公司 | 一种用于增加骨密度的组合物及其制备方法 |
| EP2702009A4 (en) | 2011-04-28 | 2015-02-18 | Calera Corp | METHODS AND COMPOSITIONS USING CALCIUM CARBONATE AND STABILIZER |
| EP2790710B1 (en) * | 2011-12-13 | 2020-08-26 | Amorphical Ltd. | Amorphous calcium carbonate for the treatment of calcium malabsorption and metabolic bone disorders |
| WO2014024191A1 (en) | 2012-08-07 | 2014-02-13 | Amorphical Ltd. | Method for producing stabilized amorphous calcium carbonate |
| CN103663532B (zh) | 2013-12-21 | 2015-10-28 | 中国科学院上海硅酸盐研究所 | 一种制备无定形碳酸钙纳米球的方法 |
| EP3174409A4 (en) | 2014-07-31 | 2018-01-17 | Amorphical Ltd. | Encapsulated amorphous calcium carbonate compositions |
| HK1253702A1 (zh) | 2015-06-04 | 2019-06-28 | 艾玛菲克有限公司 | 用聚磷酸/聚磷酸酯/聚磷酸盐或双膦酸/双膦酸酯/双膦酸盐稳定的无定形碳酸钙 |
| JP6873389B2 (ja) | 2016-01-18 | 2021-05-19 | アモーフィカル リミテッド. | 神経学的、筋肉、および不妊の疾患または症状の治療のための安定化無定形炭酸カルシウム |
| ES3052833T3 (en) | 2016-01-18 | 2026-01-15 | Amorphical Ltd | Stabilized amorphous calcium carbonate as a supplement for cell culture media |
-
2017
- 2017-10-23 JP JP2019521063A patent/JP7152785B2/ja active Active
- 2017-10-23 EP EP17863623.9A patent/EP3532074B1/en active Active
- 2017-10-23 CN CN202210530126.4A patent/CN114948992A/zh active Pending
- 2017-10-23 KR KR1020197014131A patent/KR102531595B1/ko active Active
- 2017-10-23 IL IL294615A patent/IL294615A/he unknown
- 2017-10-23 AU AU2017349921A patent/AU2017349921B2/en active Active
- 2017-10-23 IL IL266149A patent/IL266149B/he unknown
- 2017-10-23 CN CN201780080064.9A patent/CN110121351A/zh active Pending
- 2017-10-23 WO PCT/IL2017/051160 patent/WO2018078616A1/en not_active Ceased
- 2017-10-23 US US16/343,463 patent/US11052108B2/en active Active
-
2021
- 2021-06-14 US US17/346,975 patent/US20210299165A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008041236A2 (en) * | 2006-10-05 | 2008-04-10 | Ben-Gurion University Of The Negev Research And Development Authority | Composition comprising crustacean gastrolith components, calcium carbonate and its use |
| WO2009053967A1 (en) * | 2007-10-22 | 2009-04-30 | Amorphical Ltd. | Stable amorphous calcium carbonate comprising phosphorylated amino acids, synthetic phosphorylated peptides, and gastrolith proteins |
| WO2014122658A1 (en) * | 2013-02-11 | 2014-08-14 | Amorphical Ltd. | Amorphous calcium carbonate for accelerated bone growth |
Also Published As
| Publication number | Publication date |
|---|---|
| CN114948992A (zh) | 2022-08-30 |
| CN110121351A (zh) | 2019-08-13 |
| US20190262391A1 (en) | 2019-08-29 |
| KR20190073448A (ko) | 2019-06-26 |
| US11052108B2 (en) | 2021-07-06 |
| AU2017349921B2 (en) | 2023-06-15 |
| JP2019532086A (ja) | 2019-11-07 |
| IL266149A (he) | 2019-06-30 |
| JP7152785B2 (ja) | 2022-10-13 |
| EP3532074C0 (en) | 2023-08-23 |
| IL294615A (he) | 2022-09-01 |
| WO2018078616A1 (en) | 2018-05-03 |
| EP3532074A1 (en) | 2019-09-04 |
| US20210299165A1 (en) | 2021-09-30 |
| EP3532074A4 (en) | 2020-07-08 |
| KR102531595B1 (ko) | 2023-05-11 |
| EP3532074B1 (en) | 2023-08-23 |
| AU2017349921A1 (en) | 2019-06-06 |
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